Evolution and potential function of fibrinogen-like domains across twelve Drosophila species

Por Middha, Sumit, Wang, Xinguo
Publicado em 2008

From Days to Hours: Reporting Clinically Actionable Variants from Whole Genome Sequencing

Por Middha, Sumit, Baheti, Saurabh, Hart, Steven N., Kocher, Jean-Pierre A.
Publicado em 2014

Comparison of the Life Cycles of Genetically Distant Species C and Species D Human Adenoviruses Ad6 and Ad26 in Human Cells

Por Turner, Mallory A., Middha, Sumit, Hofherr, Sean E., Barry, Michael A.
Publicado no J Virol (2015)

Genomes or exomes: evaluation of cost, time and coverage

Por Middha, Sumit, Theis, Jeanne L, Goodloe, Adele H, Olson, Timothy M, Kocher, Jean-Pierre A
Publicado em 2011

A high-throughput-sequence analysis infrastructure technology investigation framework for the evaluation of next-generation sequencing software

Por Liu, Xiaoyu, Middha, Sumit, Hart, Steven, Nair, Asha, Hadad, Ahmed, Duffy, Patrick, Kocher, Jean-Pierre
Publicado em 2011

CAP-miRSeq: a comprehensive analysis pipeline for microRNA sequencing data

Por Sun, Zhifu, Evans, Jared, Bhagwate, Aditya, Middha, Sumit, Bockol, Matthew, Yan, Huihuang, Kocher, Jean-Pierre
Publicado em 2014

Novel SOD1 mutation discovered in atypical ALS by whole exome sequencing

Por Klein, Christopher J, Wu, Yanhong, Duan, Xiaohui, Middha, Sumit, Dawson, Brian D, Kocher, Jean-Pierre, Dyck, Peter J
Publicado em 2013

Histone Deacetylase Inhibition Promotes Osteoblast Maturation by Altering the Histone H4 Epigenome and Reduces Akt Phosphorylation

Por Dudakovic, Amel, Evans, Jared M., Li, Ying, Middha, Sumit, McGee-Lawrence, Meghan E., van Wijnen, Andre J., Westendorf, Jennifer J.
Publicado em 2013

Gene networks in Drosophila melanogaster: integrating experimental data to predict gene function

Por Costello, James C, Dalkilic, Mehmet M, Beason, Scott M, Gehlhausen, Jeff R, Patwardhan, Rupali, Middha, Sumit, Eads, Brian D, Andrews, Justen R
Publicado em 2009

Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome

Por Boczek, Nicole J., Best, Jabe M., Tester, David J., Giudicessi, John R., Middha, Sumit, Evans, Jared M., Kamp, Timothy J., Ackerman, Michael J.
Publicado em 2013

The molecular landscape of extraskeletal osteosarcoma: A clinicopathological and molecular biomarker study

Por Jour, George, Wang, Lu, Middha, Sumit, Zehir, Ahmet, Chen, Wen, Sadowska, Justyna, Healey, John, Agaram, Narasimhan P, Choi, Lisa, Nafa, Khedoudja, Hameed, Meera
Publicado no J Pathol Clin Res (2015)

SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencing

Por Sun, Zhifu, Baheti, Saurabh, Middha, Sumit, Kanwar, Rahul, Zhang, Yuji, Li, Xing, Beutler, Andreas S., Klee, Eric, Asmann, Yan W., Thompson, E. Aubrey, Kocher, Jean-Pierre A.
Publicado em 2012

HiChIP: a high-throughput pipeline for integrative analysis of ChIP-Seq data

Por Yan, Huihuang, Evans, Jared, Kalmbach, Mike, Moore, Raymond, Middha, Sumit, Luban, Stanislav, Wang, Liguo, Bhagwate, Aditya, Li, Ying, Sun, Zhifu, Chen, Xianfeng, Kocher, Jean-Pierre A
Publicado em 2014

Mutational Landscape of Candidate Genes in Familial Prostate Cancer

Por Johnson, Anna M., Zuhlke, Kimberly A., Plotts, Chris, McDonnell, Shannon K., Middha, Sumit, Riska, Shaun M., Thibodeau, Stephen N., Douglas, Julie A., Cooney, Kathleen A.
Publicado em 2014

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples

Por Middha, Sumit, Lindor, Noralane M., McDonnell, Shannon K., Olson, Janet E., Johnson, Kiley J., Wieben, Eric D., Farrugia, Gianrico, Cerhan, James R., Thibodeau, Stephen N.
Publicado no Front Genet (2015)

Research Resource: Whole Transcriptome RNA Sequencing Detects Multiple 1α,25-Dihydroxyvitamin D(3)-Sensitive Metabolic Pathways in Developing Zebrafish

Por Craig, Theodore A., Zhang, Yuji, McNulty, Melissa S., Middha, Sumit, Ketha, Hemamalini, Singh, Ravinder J., Magis, Andrew T., Funk, Cory, Price, Nathan D., Ekker, Stephen C., Kumar, Rajiv
Publicado em 2012

Ubiquitin ligase defect by DCAF8 mutation causes HMSN2 with giant axons

Por Klein, Christopher J., Wu, Yanhong, Vogel, Peter, Goebel, Hans H., Bönnemann, Carsten, Zukosky, Kristen, Botuyan, Maria-Victoria, Duan, Xiaohui, Middha, Sumit, Atkinson, Elizabeth J., Mer, Georges, Dyck, Peter J.
Publicado em 2014

Comprehensive Assessment of Genetic Variants Within TCF4 in Fuchs' Endothelial Corneal Dystrophy

Por Wieben, Eric D., Aleff, Ross A., Eckloff, Bruce W., Atkinson, Elizabeth J., Baheti, Saurabh, Middha, Sumit, Brown, William L., Patel, Sanjay V., Kocher, Jean-Pierre A., Baratz, Keith H.
Publicado em 2014

Comprehensively Evaluating cis-Regulatory Variation in the Human Prostate Transcriptome by Using Gene-Level Allele-Specific Expression

Por Larson, Nicholas B., McDonnell, Shannon, French, Amy J., Fogarty, Zach, Cheville, John, Middha, Sumit, Riska, Shaun, Baheti, Saurabh, Nair, Asha A., Wang, Liang, Schaid, Daniel J., Thibodeau, Stephen N.
Publicado no Am J Hum Genet (2015)

Identification of Targetable Kinase Alterations in Patients with Colorectal Carcinoma That are Preferentially Associated with Wild-Type RAS/RAF

Por Hechtman, Jaclyn F., Zehir, Ahmet, Yaeger, Rona, Wang, Lu, Middha, Sumit, Zheng, Tao, Hyman, David M., Solit, David, Arcila, Maria E., Borsu, Laetitia, Shia, Jinru, Vakiani, Efsevia, Saltz, Leonard, Ladanyi, Marc
Publicado no Mol Cancer Res (2015)